US5049314A - Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate - Google Patents

Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate Download PDF

Info

Publication number
US5049314A
US5049314A US07/675,286 US67528691A US5049314A US 5049314 A US5049314 A US 5049314A US 67528691 A US67528691 A US 67528691A US 5049314 A US5049314 A US 5049314A
Authority
US
United States
Prior art keywords
paint
composition
weight
pyrrolidone
ethyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US07/675,286
Inventor
Sidney M. Short
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
MARGARET VILLA Inc
Original Assignee
Chute Chemical Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Chute Chemical Co filed Critical Chute Chemical Co
Priority to US07/675,286 priority Critical patent/US5049314A/en
Application granted granted Critical
Publication of US5049314A publication Critical patent/US5049314A/en
Assigned to MARGARET VILLA INC. reassignment MARGARET VILLA INC. ASSIGNMENT OF ASSIGNORS INTEREST (SEE DOCUMENT FOR DETAILS). Assignors: CHUTE CHEMICAL COMPANY
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D9/00Chemical paint or ink removers
    • C09D9/005Chemical paint or ink removers containing organic solvents
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/43Solvents

Definitions

  • the present invention relates to a paint stripping composition used in a process where it is applied to a substrate coated with fully or partially cured paint.
  • the composition of the present invention has particular utility for use in stripping paint and will be described in connection with such utility, although other utilities, for example, stripping organic polymer coatings, also are contemplated.
  • the present invention is also directed to a method of employing the stripping composition.
  • a paint or varnish remover should ideally remove all traces of the coating quickly and with a minimum of labor, and it should leave the substrate unharmed and suitable for reprocessing or refinishing.
  • a number of design criteria have been identified for a modern stripper: stripping ability, lack of corrosiveness to substrates, freedom from galvanic attack at the juncture of dissimilar materials, freedom from noxious and toxic chemicals, good shelf life, high viscosity, where needed, sealable internally or with a water cap to prevent rapid evaporation, and ability to leave a readily recoatable surface. See The Encyclopedia of Chemical Technology, Third Edition, Volume 16, 762-768 (1981).
  • Methylene chloride paint strippers have long been the industry standard for paint stripper performance. It has been established that methylene chloride is effective for quickly softening most types of paints. It has been suggested that the effectiveness of methylene chloride results from its smaller molecular size. Its low molecular weight enables it to penetrate rapidly into a coating, and its intermediate solvency enables the coating not to be dissolved so that redisposition on the substrate is avoided. Methylene chloride removers have also been modified to increase stripping power for special purposes. These modifying chemicals include amines, alkalies and organic acids. See U.S. Pat. No. 3,538,007 to Cooper et. al. Other reported uses of methylene chloride include solvent degreasing, plastics processing, blowing agent in foams, solvent extraction, a solvent for cellulose acetate, and as an aerosol propellant.
  • methylene chloride has now been closely regulated for environmental protection. Recently, it was discovered that methylene chloride can cause tumors in rats and mice. The LD 50 orally in rats (young adults) has been found to be 1.6 ml/kg. Furthermore, the threshold limiting value (TLV) has been set at 100 ppm in air. See Kimura, et. al., Toxicol. Appl. Pharmacol. 19, 699 (1971). Since these discoveries, the wide use of the solvent by industry and consumers has come under close scrutiny by federal regulatory agencies. See, U.S. Pat. No. 4,749,510 to Nelson. Accordingly, it is now highly desirable to avoid the use of methylene chloride in paint stripping formulations.
  • FDA Food and Drug Administration
  • NMP N-methyl-2-pyrrolidone
  • NMP is less toxic than many competitive aprotic solvents and does not appear to be a sensitizing agent.
  • NMP a dipolar aprotic solvent
  • NMP has a high dielectric constant and cannot donate protons for hydrogen bonding. Consequently, many of its applications involve its strong and frequently selective solvating power.
  • NMP is commercially available (e.g., from BASF Wyandotte or GAF) and used industrially as a processing aid for polymeric resins, in petroleum processing (e.g., the extraction of aromatics from lube oil), for the production of electronic circuitry, and as a general industrial cleaning ingredient.
  • NMP is a colorless liquid with a mild amine odor, is miscible with water as well as various organic solvents. See the Encyclopedia of Chemical Technology, Third Edition, Vol. 19, 514-520 (1981).
  • NMP was recognized as an early candidate for replacing chlorinated solvent type paint strippers, it was soon discovered that a formulation based entirely on NMP had a number of disadvantages.
  • NMP has low viscosity and low adhesive properties which work against its efficiency to remove dried coats of paint on a vertical surface.
  • a NMP composition is reported where a viscosifying agent (rhamsan gum) is added to the NMP to improve the ability of the composition to cling to a painted surface when inclined in a vertical position.
  • rhamsan gum rhamsan gum
  • Another object is the provision of a stripper of the above type which can be applied by any conventional method, including wetting, wiping, spraying, brushing, dipping, troweling or otherwise.
  • Yet another object is to provide an effective composition with the aforementioned properties for cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete.
  • a still further object is to provide a stripper composition of the above type which emulsifies with and can be completely removed by water.
  • a stripper composition which comprises essentially of a mixture of the two following essential components: (1) a five-membered ring lactam, and (2) an oxygenated aliphatic solvent.
  • the composition preferably also contains certain other components including a thickener, preferably a cellulose ether derivative such as hydroxy propyl cellulose, a conventional surfactant, preferably tridecylalcohol-6-mole-ethoxylate, corrosion inhibitors, dyes and fragrances. All of these additional components are employed in effective amounts, particularly in certain ranges of proportions, as set forth in greater detail below.
  • a thickener preferably a cellulose ether derivative such as hydroxy propyl cellulose
  • a conventional surfactant preferably tridecylalcohol-6-mole-ethoxylate
  • corrosion inhibitors preferably tridecylalcohol-6-mole-ethoxylate
  • dyes preferably tridecylalcohol-6-mole-ethoxylate
  • the inventive composition is particularly effective for stripping and cleaning of paints, coatings, inks and crayon as well as cleaning some urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete.
  • the paint stripper composition of the invention is readily formulated from commercially available solvents and applied by any conventional method, including wetting, wiping, spraying, brushing, dipping, troweling or otherwise. The paint or coating is removed easily without any substantial waiting or soaking, followed by water rinsing to clean the removed paint.
  • the paint/coatings stripper hereof readily emulsifies with water and is removed completely by water.
  • the stripper composition of the invention is essentially non-flammable, non-carcinogenic, and non-toxic.
  • NMP N-methyl-2-pyrrolidone
  • NMP N-methyl-2-pyrrolidone
  • other hydrocarbon 2-pyrrolidones for example, N-ethyl-2-pyrrolidone, N-isopropyl-2-pyrrolidone, N-cyclohexyl-2-pyrrolidone, 2-hydroxyethyl-2-pyrrolidone, N-dimethylaminopropyl -2-pyrrolidone, vinyl-pyrrolidone, 2-pyrrolidone and mixtures thereof.
  • NMP is a cyclic amide having a flashpoint (open-cup) of 95° C.
  • the chemical formula for NMP is C 5 H 9 NO.
  • the second essential component of the present invention is an oxygenated aliphatic solvent.
  • esters of propionic acid in particular the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, 3-methylbutyl, pentyl, hexyl, heptyl, octyl esters of propionic acid, and mixtures of the foregoing.
  • Particularly preferred is ethyl-3-ethoxypropionate which when combined with NMP provides the two primary constituents in the paint/coatings stripper composition of the present invention.
  • oxygenated solvents useful in the present invention which may be used in mixture with or as a substitution for the aforesaid esters of propionic acid are mentioned aliphatic alcohols such as butyl alcohol, amyl alcohol, hexyl alcohol, heptyl alcohol, furfuryl alcohol, tetrahydrofurfuryl alcohol, 2-butoxy ethanol; 2 or 3 carbon atom; alkylene glycol ethers such as propylene glycol mono-t-butyl ether, dipropylene glycol mono-methyl ether, and dipropylene gylcol mono-n-butyl ether; 6 to 8 carbon atom; aliphatic dibasic esters such as dimethyl succinate, dimethyl glutarate and dimethyl adipate; and aliphatic ketones such as diisobutyl ketone.
  • aliphatic alcohols such as butyl alcohol, amyl alcohol, hexyl alcohol, heptyl alcohol, furfuryl alcohol,
  • each of the two essential components in the final composition may vary within a certain range. What is important, however, is that each be present in an amount sufficient to provide the composition with effectiveness for stripping and cleaning of paints, coatings, inks and crayon as well as cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete. Therefore, in accordance with the broad principles of this invention, the combination of the two essential components from the above mentioned classes is achieved by a consideration of the solvating capacities of the respective components, individually and in combination, in order to obtain the most desired biodegradable, least flammable and highest threshold limiting values to meet or exceed health and safety standards.
  • the composition may contain from about 10-90% of the five-membered ring lactam, preferably from about 20-40%, and in the most preferred embodiment about 30-35% by weight of the paint stripper composition.
  • the other essential component i.e., the oxygenated aliphatic solvent, may be present in the composition from about 10-90% preferably from about 55-75%, and in the most preferred embodiment about 65-70% by weight of the paint stripper composition.
  • Surface active agents also may be utilized in the composition. These compounds tend to reduce the surface tension when dissolved in water or water solutions, or reduce interfacial tension between two liquids, or between a liquid and a solid. Therefore, in the context of the paint stripping formulations of the present invention, which is water soluble, the surface active agents serve to make the various stripping formulations amenable to water flushing from the treated surface. That is, when the assorted formulations of this invention are applied to non-water soluble paints and coatings, along with surface-active agents, such agents are further believed to effect an emulsion of the organic residues that have been removed from the various substrates on contact with water. Such emulsions can then be rinsed from the treated surface with water.
  • Surface-active agents may be of four types, nonionic, anionic, cationic or amphoteric. They are selected for solubility in the stripping formulation, low toxicity, the ability to form a useful emulsion of the formula with water, and biodegradability. Normally, if surface-active agents are included in the formulation, they are included in the amount from about 1 to 8 weight percent, and preferably from about 3 to 6 weight percent.
  • a preferred embodiment of the present invention includes an oil soluble nonionic surfactant, the 6-mole ethoxylate of tridecyl alcohol which is available from GAF under the tradename Emulphogene 610, and from Stepan under the tradename Makon TD-6.
  • Corrosion inhibitors may also be included in the inventive formulation. Such corrosion inhibitors are conventional. Typical corrosion inhibitors include mono-, di-, and triethanol amines as well as many solvent soluble commercial preparations Other acceptable amines include diethylethanolamine, diisopropylamine, ethylamine, ethylenediamine, isopropylamine, monoisopropanolamine, morpholine, triethylenetetramine, and triisopropynolamine. Mixtures of such alkanolamines can be employed when desired.
  • the preferred thickeners or gelling agents are cellulose derivatives having the property of both water and organic solvent solubility.
  • Cellulose derivatives of this type which are of particular interest are those ether derivatives containing etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, such etherifying groups containing preferably up to about 5 or 6 carbon atoms.
  • the gelling agent also may comprise cellulose ether derivatives which, in addition to etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, contain other types of etherifying groups, especially small alkyl groups of, for example, one or two carbon atoms.
  • such etherifying groups generally confer properties upon the cellulose derivative which are less acceptable for the present purpose, and the gelling agent is therefore conveniently substantially restricted to cellulose derivatives containing the etherifying groups selected from the hydroxyalkyl groups and groups derived therefrom.
  • Etherifying groups consisting of or derived from hydroxyalkyl groups containing up to 5 carbon atoms, particularly, 2, 3 or 4 carbon atoms, are of especial value.
  • the hydroxypropyl celluloses for example, have been found to be of particular value in imparting quite adequate thickening properties in their own right without the need for any other agents for these purposes.
  • the hydroxypropyl group in these cellulose derivatives may be derived from either isopropanol or n-propanol and a number of variations are possible. For any etherification of cellulose, not all of the free hydroxy groups on the cellulose need necessarily be substituted.
  • any free hydroxy groups, and the hydroxypropyl group itself, may be further substituted by treatment with other aliphatic alcohols.
  • the hydroxypropyl celluloses employed in formulations according to the present invention have molecular weights in the range of 50,000 to about 1,000,000, preferably from about 800,000 to 1,000,000. Since the molecular weight of these described thickeners is directly proportional to their ability to alter the viscosity of a given formulation, the concentrations that are preferred for a desired viscosifying effect will vary depending on the molecular weight selected. The proportions of thickener in the formulations can be in the range of 0.25% to 10%, or even 15%, 18% or 20% by weight.
  • the usual proportion of thickening agent of from about 0.25% or 0.5% upwards is suitable for high molecular weight materials and of from about 3% upwards being suitable for lower molecular weight materials.
  • high molecular weight materials for example molecular weights of 800,000 to 1,000,000 a proportion of above 1.5% is preferably avoided as it leads to a viscosifying effect of too large a magnitude.
  • low molecular weight materials larger proportions may be used before such a position is reached and, if the molecular weight is low enough, amounts of up to 10% or even 20% or more may be used. It will be appreciated, however, that the use of a smaller amount of material of high molecular weight is generally to be preferred.
  • Dyes and fragrances can be selected according to the needs of product identification as well as aesthetics.
  • the appropriate dye or fragrance should be chemically stable in the formulations, as well as having little or no effect on the ability of the given formulation to effect removal of the paint or coating from the substrate.
  • the dye or fragrance should have little to no effect on the ability of the surface-active agent to create an emulsion so that rinsability with water is maintained.
  • only a small amount of such a dye or fragrance will be employed, from about 0.001% to 0.1% by weight of the entire formulation.
  • Typical of such dyes are are Pylaklor LX-1911A Orange which is available from Pylam. Any commercially available fragrance may be employed.
  • the formulation of this invention is prepared by first vigorously mixing the oxygenated aliphatic hydrocarbon solvent as the thickener is sifted over the surface of the solvent which then forms a fine uniform miscible mixture forming a gel.
  • the thickener is added extremely slowly to permit the thickener to dissolve without forming a precipitate or large agglomeration.
  • the extremely slow rate of addition of the thickener to the mixture is required due to the relative incompatibility of some of the cellulose ether derivatives. If some of the cellulose ethers are added too quickly, a precipitate or agglomeration will form and the cellulose ether will not function as a thickening agent for the paint/coatings stripper.
  • the corrosion inhibitors, dyes, fragrances and lactone are added to the oxygenated alphatic solvent and cellulose ether, followed by the appropriate surface-active agent or mixture of surface-active agents.
  • the resulting formulation of the invention is used, preferably undiluted for removing paint or coatings from a substrate.
  • the formulation may be applied to the paint or coated surface by spraying, brushing, dipping, troweling, or otherwise.
  • the paint or coating on the surface is then softened by the reaction with lactam and the oxygenated aliphatic solvent and is held in suspension on the surface by the thickener, if present.
  • the stripper and loosened paint may be rinsed from the surface with water or manually scraped or sanded from the substrate.
  • the paint stripper normally requires 1 to 30 minutes to soften the paint on the substrate, depending on the type of paint.
  • the resultant paint stripper removed paint as rapidly as NMP does alone and is significantly less expensive than NMP.
  • the time required to completely strip cured and partially cured paint was about 1-5 minutes, depending on the type of paint, and only a single application was required.
  • the paint on the surface was degraded and lifted off the substrate.
  • it also removed lipstick and crayon much faster than NMP which makes this formula highly desirable for removing graffiti when the composition of the graffiti is unknown.
  • the composition is highly biodegradable as demonstrated by the following data:
  • This example produces a high viscosity composition which is highly effective for stripping vertical surfaces. More particularly, water emulsions prepared with this formula are more stable than those made with Example 1.
  • Example 3 removed paint equally as fast as the formulation of Example 1, and has the advantage that it leaves no residue on air drying, and thus may advantageously be employed in the electronics industry. On the other hand, the formulation of Examples 1 and 2 will not adhere.
  • the composition has a long work life which typically permits complete removal from the substrate with a single application regardless of the thickness of the paint accumulation. In most instances, since the stripper can be left on until all the paint is loosened. Indeed, many coatings will totally dissolve if soaked. This is a significant advantage of the present invention as compared to methylene chloride paint strippers.
  • the paints upon which the paint stripper of the present invention is effective include those conventionally used as automotive touch-up paints, metal enamels, lacquers, varnishes, polymer paints and others used in industrial processes and also general purpose household paints and surface coatings.
  • the stripping formulations of this invention can remove many of the dyes and pigments associated with lipstick and crayon formulations which makes this formulation highly desirable for removing graffiti where the composition of the graffiti is unknown.
  • the stripping composition of the present invention also can be applied to reactive-vehicle or solvent borne coatings, and has also proven effective for cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly if applied before the cure is complete.
  • composition also may be emulsified with water and remain effective on many latex coatings.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Materials Engineering (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Paints Or Removers (AREA)
  • Detergent Compositions (AREA)

Abstract

A paint stripping composition used in a process where it is applied to a substrate coated with fully or partially cured paint, having particular utility for use in stripping paint with other utilities, e.g. stripping organic polymer coatings also contemplated, and a method of employing same is described.

Description

BACKGROUND OF THE INVENTION
1. Technical Field
The present invention relates to a paint stripping composition used in a process where it is applied to a substrate coated with fully or partially cured paint. The composition of the present invention has particular utility for use in stripping paint and will be described in connection with such utility, although other utilities, for example, stripping organic polymer coatings, also are contemplated. The present invention is also directed to a method of employing the stripping composition.
2. Brief Description of the Background Art
A paint or varnish remover should ideally remove all traces of the coating quickly and with a minimum of labor, and it should leave the substrate unharmed and suitable for reprocessing or refinishing. A number of design criteria have been identified for a modern stripper: stripping ability, lack of corrosiveness to substrates, freedom from galvanic attack at the juncture of dissimilar materials, freedom from noxious and toxic chemicals, good shelf life, high viscosity, where needed, sealable internally or with a water cap to prevent rapid evaporation, and ability to leave a readily recoatable surface. See The Encyclopedia of Chemical Technology, Third Edition, Volume 16, 762-768 (1981).
Methylene chloride paint strippers have long been the industry standard for paint stripper performance. It has been established that methylene chloride is effective for quickly softening most types of paints. It has been suggested that the effectiveness of methylene chloride results from its smaller molecular size. Its low molecular weight enables it to penetrate rapidly into a coating, and its intermediate solvency enables the coating not to be dissolved so that redisposition on the substrate is avoided. Methylene chloride removers have also been modified to increase stripping power for special purposes. These modifying chemicals include amines, alkalies and organic acids. See U.S. Pat. No. 3,538,007 to Cooper et. al. Other reported uses of methylene chloride include solvent degreasing, plastics processing, blowing agent in foams, solvent extraction, a solvent for cellulose acetate, and as an aerosol propellant.
The safe use of methylene chloride has been questioned by Federal agencies including the Food and Drug Administration (FDA). As a chlorinated solvent, methylene chloride has now been closely regulated for environmental protection. Recently, it was discovered that methylene chloride can cause tumors in rats and mice. The LD50 orally in rats (young adults) has been found to be 1.6 ml/kg. Furthermore, the threshold limiting value (TLV) has been set at 100 ppm in air. See Kimura, et. al., Toxicol. Appl. Pharmacol. 19, 699 (1971). Since these discoveries, the wide use of the solvent by industry and consumers has come under close scrutiny by federal regulatory agencies. See, U.S. Pat. No. 4,749,510 to Nelson. Accordingly, it is now highly desirable to avoid the use of methylene chloride in paint stripping formulations.
The search for an alternative product to methylene chloride has focused attention on pyrrolidone type compounds, more specifically, N-methyl-2-pyrrolidone (NMP). NMP is less toxic than many competitive aprotic solvents and does not appear to be a sensitizing agent. NMP, a dipolar aprotic solvent, has a high dielectric constant and cannot donate protons for hydrogen bonding. Consequently, many of its applications involve its strong and frequently selective solvating power. NMP is commercially available (e.g., from BASF Wyandotte or GAF) and used industrially as a processing aid for polymeric resins, in petroleum processing (e.g., the extraction of aromatics from lube oil), for the production of electronic circuitry, and as a general industrial cleaning ingredient. NMP is a colorless liquid with a mild amine odor, is miscible with water as well as various organic solvents. See the Encyclopedia of Chemical Technology, Third Edition, Vol. 19, 514-520 (1981).
Although NMP was recognized as an early candidate for replacing chlorinated solvent type paint strippers, it was soon discovered that a formulation based entirely on NMP had a number of disadvantages.
For example, NMP has low viscosity and low adhesive properties which work against its efficiency to remove dried coats of paint on a vertical surface. In U.S. Pat. No. 4,764,222 to Colegrove, a NMP composition is reported where a viscosifying agent (rhamsan gum) is added to the NMP to improve the ability of the composition to cling to a painted surface when inclined in a vertical position. An effort to optimize or target the paint removing efficiency and water solubility of NMP, while at the same time controlling and minimizing any potential toxicity and volatility, has led to a variety of specific formulations combining NMP with other organic and inorganic compounds. In U.S. Pat. No. 4,276,186 to Bakos et. al , cleaning compositions containing at least 50% by weight of NMP and at least about 5% by weight of a water miscible alkanolamine and about 0-35% by weight of a hydrocarbon solvent were described as especially suitable for removing solder flux from a ceramic substrate. In U.S. Pat. No. 4,664,721 to Valasek, non-aqueous compositions of NMP, butyl cellosolve and cyclohexanone and a surfactant are disclosed which degraded or solubilized broad classes of printing ink residues on printing screens. In U.S. Pat. No. 4,812,255 to Suwala, an aliphatic organic acid, an alkylene glycol ether and NMP are combined and reported effective as an overall composition for paint removal. In U.S. Pat. No. 4,732,695 to Francisco, a paint stripper and coatings remover composition consisted of three essential components: NMP, a mixture of aromatic hydrocarbons and benzyl alcohol. Finally, in U.S. Pat. No. 4,749,510 to Nelson, there is described a paint stripping composition comprising about 20-90% by weight NMP, 30-70% by weight aromatic hydrocarbon solvent, and about 1-15% by weight of either formic, oxalic, acetic, citric, gluconic or glutamic acid. According to another aspect of Nelson, organic amines such as diethanol amine could replace the various organic acids.
The combination of NMP with a variety of operative organic compounds represents what has been a long-standing effort to maximize the stripping ability of this alternative paint and coatings remover. While some of the presently disclosed paint strippers have relied upon formulations and proportions of active organic compounds in combination with NMP, none have recognized the novel and enhanced solvating power of the present invention which utilizes components that are commercially widely available, are less expensive than NMP, remove certain paints, coatings, inks or crayon at the same or better rate than NMP alone, can replace the majority of NMP in a given formulation, and are biodegradable, non-flammable and non-toxic.
It is accordingly an object of the present invention to provide an effective non-methylene chloride paint stripper composition that can be readily mixed and formulated to produce a stripper with the aforementioned solvating capability.
Another object is the provision of a stripper of the above type which can be applied by any conventional method, including wetting, wiping, spraying, brushing, dipping, troweling or otherwise.
Yet another object is to provide an effective composition with the aforementioned properties for cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete.
A still further object is to provide a stripper composition of the above type which emulsifies with and can be completely removed by water.
SUMMARY OF THE INVENTION
The above and other objects and advantages are achieved by a stripper composition which comprises essentially of a mixture of the two following essential components: (1) a five-membered ring lactam, and (2) an oxygenated aliphatic solvent.
The composition preferably also contains certain other components including a thickener, preferably a cellulose ether derivative such as hydroxy propyl cellulose, a conventional surfactant, preferably tridecylalcohol-6-mole-ethoxylate, corrosion inhibitors, dyes and fragrances. All of these additional components are employed in effective amounts, particularly in certain ranges of proportions, as set forth in greater detail below.
The inventive composition is particularly effective for stripping and cleaning of paints, coatings, inks and crayon as well as cleaning some urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete. The paint stripper composition of the invention is readily formulated from commercially available solvents and applied by any conventional method, including wetting, wiping, spraying, brushing, dipping, troweling or otherwise. The paint or coating is removed easily without any substantial waiting or soaking, followed by water rinsing to clean the removed paint. The paint/coatings stripper hereof readily emulsifies with water and is removed completely by water. As formulated the stripper composition of the invention is essentially non-flammable, non-carcinogenic, and non-toxic.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
One of the two essential components in the paint and coatings stripper formulation of the present invention is a five-membered ring lactone. Preferred in this group is N-methyl-2-pyrrolidone (NMP), as well as other hydrocarbon 2-pyrrolidones, for example, N-ethyl-2-pyrrolidone, N-isopropyl-2-pyrrolidone, N-cyclohexyl-2-pyrrolidone, 2-hydroxyethyl-2-pyrrolidone, N-dimethylaminopropyl -2-pyrrolidone, vinyl-pyrrolidone, 2-pyrrolidone and mixtures thereof. Particularly preferred is NMP which is a cyclic amide having a flashpoint (open-cup) of 95° C. The chemical formula for NMP is C5 H9 NO.
The second essential component of the present invention is an oxygenated aliphatic solvent. Preferred are esters of propionic acid, in particular the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, 3-methylbutyl, pentyl, hexyl, heptyl, octyl esters of propionic acid, and mixtures of the foregoing. Particularly preferred is ethyl-3-ethoxypropionate which when combined with NMP provides the two primary constituents in the paint/coatings stripper composition of the present invention. Amongst other oxygenated solvents useful in the present invention which may be used in mixture with or as a substitution for the aforesaid esters of propionic acid are mentioned aliphatic alcohols such as butyl alcohol, amyl alcohol, hexyl alcohol, heptyl alcohol, furfuryl alcohol, tetrahydrofurfuryl alcohol, 2-butoxy ethanol; 2 or 3 carbon atom; alkylene glycol ethers such as propylene glycol mono-t-butyl ether, dipropylene glycol mono-methyl ether, and dipropylene gylcol mono-n-butyl ether; 6 to 8 carbon atom; aliphatic dibasic esters such as dimethyl succinate, dimethyl glutarate and dimethyl adipate; and aliphatic ketones such as diisobutyl ketone. While such other solvents provide a formulation which is relatively non-toxic, the speed of paint removal is not as great as when using ethyl-3 -ethoxypropionate. It has been observed that up to 50% of the ethyl-3-ethoxypropionate may be replaced by 2-butoxyethanol with little or no apparent sacrifice in paint removal performance; however, 2-butoxyethanol is not preferred since it has been suspected of having toxic properties.
The amount of each of the two essential components in the final composition may vary within a certain range. What is important, however, is that each be present in an amount sufficient to provide the composition with effectiveness for stripping and cleaning of paints, coatings, inks and crayon as well as cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly before the cure is complete. Therefore, in accordance with the broad principles of this invention, the combination of the two essential components from the above mentioned classes is achieved by a consideration of the solvating capacities of the respective components, individually and in combination, in order to obtain the most desired biodegradable, least flammable and highest threshold limiting values to meet or exceed health and safety standards. Typically, the composition may contain from about 10-90% of the five-membered ring lactam, preferably from about 20-40%, and in the most preferred embodiment about 30-35% by weight of the paint stripper composition. The other essential component, i.e., the oxygenated aliphatic solvent, may be present in the composition from about 10-90% preferably from about 55-75%, and in the most preferred embodiment about 65-70% by weight of the paint stripper composition.
Surface active agents also may be utilized in the composition. These compounds tend to reduce the surface tension when dissolved in water or water solutions, or reduce interfacial tension between two liquids, or between a liquid and a solid. Therefore, in the context of the paint stripping formulations of the present invention, which is water soluble, the surface active agents serve to make the various stripping formulations amenable to water flushing from the treated surface. That is, when the assorted formulations of this invention are applied to non-water soluble paints and coatings, along with surface-active agents, such agents are further believed to effect an emulsion of the organic residues that have been removed from the various substrates on contact with water. Such emulsions can then be rinsed from the treated surface with water.
Surface-active agents may be of four types, nonionic, anionic, cationic or amphoteric. They are selected for solubility in the stripping formulation, low toxicity, the ability to form a useful emulsion of the formula with water, and biodegradability. Normally, if surface-active agents are included in the formulation, they are included in the amount from about 1 to 8 weight percent, and preferably from about 3 to 6 weight percent. A preferred embodiment of the present invention includes an oil soluble nonionic surfactant, the 6-mole ethoxylate of tridecyl alcohol which is available from GAF under the tradename Emulphogene 610, and from Stepan under the tradename Makon TD-6.
Corrosion inhibitors may also be included in the inventive formulation. Such corrosion inhibitors are conventional. Typical corrosion inhibitors include mono-, di-, and triethanol amines as well as many solvent soluble commercial preparations Other acceptable amines include diethylethanolamine, diisopropylamine, ethylamine, ethylenediamine, isopropylamine, monoisopropanolamine, morpholine, triethylenetetramine, and triisopropynolamine. Mixtures of such alkanolamines can be employed when desired.
For stripping vertical surfaces the addition of a thickener or gelling agent is highly desirable. The preferred thickeners or gelling agents are cellulose derivatives having the property of both water and organic solvent solubility. Cellulose derivatives of this type which are of particular interest are those ether derivatives containing etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, such etherifying groups containing preferably up to about 5 or 6 carbon atoms. The gelling agent also may comprise cellulose ether derivatives which, in addition to etherifying groups selected from hydroxyalkyl groups and groups derived therefrom, contain other types of etherifying groups, especially small alkyl groups of, for example, one or two carbon atoms. However, such etherifying groups generally confer properties upon the cellulose derivative which are less acceptable for the present purpose, and the gelling agent is therefore conveniently substantially restricted to cellulose derivatives containing the etherifying groups selected from the hydroxyalkyl groups and groups derived therefrom.
Etherifying groups consisting of or derived from hydroxyalkyl groups containing up to 5 carbon atoms, particularly, 2, 3 or 4 carbon atoms, are of especial value. The hydroxypropyl celluloses, for example, have been found to be of particular value in imparting quite adequate thickening properties in their own right without the need for any other agents for these purposes. The hydroxypropyl group in these cellulose derivatives may be derived from either isopropanol or n-propanol and a number of variations are possible. For any etherification of cellulose, not all of the free hydroxy groups on the cellulose need necessarily be substituted. Consequently any free hydroxy groups, and the hydroxypropyl group itself, may be further substituted by treatment with other aliphatic alcohols. The hydroxypropyl celluloses employed in formulations according to the present invention have molecular weights in the range of 50,000 to about 1,000,000, preferably from about 800,000 to 1,000,000. Since the molecular weight of these described thickeners is directly proportional to their ability to alter the viscosity of a given formulation, the concentrations that are preferred for a desired viscosifying effect will vary depending on the molecular weight selected. The proportions of thickener in the formulations can be in the range of 0.25% to 10%, or even 15%, 18% or 20% by weight. Thus, for example, the usual proportion of thickening agent of from about 0.25% or 0.5% upwards is suitable for high molecular weight materials and of from about 3% upwards being suitable for lower molecular weight materials. For high molecular weight materials, for example molecular weights of 800,000 to 1,000,000 a proportion of above 1.5% is preferably avoided as it leads to a viscosifying effect of too large a magnitude. With low molecular weight materials, larger proportions may be used before such a position is reached and, if the molecular weight is low enough, amounts of up to 10% or even 20% or more may be used. It will be appreciated, however, that the use of a smaller amount of material of high molecular weight is generally to be preferred.
Dyes and fragrances can be selected according to the needs of product identification as well as aesthetics. The appropriate dye or fragrance should be chemically stable in the formulations, as well as having little or no effect on the ability of the given formulation to effect removal of the paint or coating from the substrate. Furthermore, the dye or fragrance should have little to no effect on the ability of the surface-active agent to create an emulsion so that rinsability with water is maintained. Preferably, only a small amount of such a dye or fragrance will be employed, from about 0.001% to 0.1% by weight of the entire formulation. Typical of such dyes are are Pylaklor LX-1911A Orange which is available from Pylam. Any commercially available fragrance may be employed.
WORKING EXAMPLES
The following examples, illustrative of the present invention, involve: mixing of the constituents together by blending with a mechanical mixer in a tank or other similar vessel. The formulation of this invention is prepared by first vigorously mixing the oxygenated aliphatic hydrocarbon solvent as the thickener is sifted over the surface of the solvent which then forms a fine uniform miscible mixture forming a gel. The thickener is added extremely slowly to permit the thickener to dissolve without forming a precipitate or large agglomeration. The extremely slow rate of addition of the thickener to the mixture is required due to the relative incompatibility of some of the cellulose ether derivatives. If some of the cellulose ethers are added too quickly, a precipitate or agglomeration will form and the cellulose ether will not function as a thickening agent for the paint/coatings stripper.
Next, the corrosion inhibitors, dyes, fragrances and lactone are added to the oxygenated alphatic solvent and cellulose ether, followed by the appropriate surface-active agent or mixture of surface-active agents.
The resulting formulation of the invention is used, preferably undiluted for removing paint or coatings from a substrate. The formulation may be applied to the paint or coated surface by spraying, brushing, dipping, troweling, or otherwise. The paint or coating on the surface is then softened by the reaction with lactam and the oxygenated aliphatic solvent and is held in suspension on the surface by the thickener, if present. After the paint or coating is softened, the stripper and loosened paint may be rinsed from the surface with water or manually scraped or sanded from the substrate. The paint stripper normally requires 1 to 30 minutes to soften the paint on the substrate, depending on the type of paint.
EXAMPLE 1
Following the procedure set forth above, the following formulation was prepared:
______________________________________                                    
Constituent        % by Weight                                            
______________________________________                                    
N-methyl-2-pyrrolidone                                                    
                   29.9                                                   
(NMP)                                                                     
Ethyl-3-ethoxypropionate                                                  
                   65.0                                                   
6-mole ethoxylate of                                                      
                   5.0                                                    
tridecyl alcohol                                                          
Fragrance          0.1                                                    
Dye (Pylaklor LX-1911A                                                    
                   0.001                                                  
Orange)                                                                   
______________________________________                                    
The resultant paint stripper removed paint as rapidly as NMP does alone and is significantly less expensive than NMP. The time required to completely strip cured and partially cured paint was about 1-5 minutes, depending on the type of paint, and only a single application was required. The paint on the surface was degraded and lifted off the substrate. Furthermore, it also removed lipstick and crayon much faster than NMP which makes this formula highly desirable for removing graffiti when the composition of the graffiti is unknown. The composition is highly biodegradable as demonstrated by the following data:
______________________________________                                    
Chemical Oxygen Demand = 1.71 kg/kg                                       
Biological O.sub.2                                                        
             Concentration Tested                                         
Demand (kg/kg/%)                                                          
             2 mg/l.   5 mg/l.    10 mg/l.                                
______________________________________                                    
Day  5      0.550/32.2%                                                   
                       0.610/35.9%                                        
                                  0.720/42.1%                             
Day 10      0.700/40.9%                                                   
                       0.740/43.3%                                        
                                  Septic                                  
Day 15      0.950/55.6%                                                   
                        1.00/58.5%                                        
                                  Septic                                  
Day 20       1.20/70.0%                                                   
                       Septic     Septic                                  
______________________________________                                    
The above tests were run by an independent laboratory using an unacclimated municipal seed. The fact that higher concentrations biodegraded faster and went septic indicates that the inventive formulations have no toxicity to treatment plant organisms. The % biodegradation is the BOD/COD multiplied by 100.
EXAMPLE 2
Following the procedure set forth above, the following formulation was prepared:
______________________________________                                    
Constituent        % by Weight                                            
______________________________________                                    
NMP                29.9                                                   
Ethyl-3-ethoxypropionate                                                  
                   64.0                                                   
6-mole ethoxylate of                                                      
                   5.0                                                    
tridecyl alcohol                                                          
High Viscosity hydroxy-                                                   
                   1.0                                                    
propyl cellulose                                                          
Fragrance          0.1                                                    
Dye (Pylaklor LX-1911A                                                    
                   0.001                                                  
Orange)                                                                   
______________________________________                                    
This example produces a high viscosity composition which is highly effective for stripping vertical surfaces. More particularly, water emulsions prepared with this formula are more stable than those made with Example 1.
EXAMPLE 3
Following the procedure set forth above, the following formulation was prepared:
______________________________________                                    
Constituent        % by Weight                                            
______________________________________                                    
NMP                30.0                                                   
Ethyl-3-ethoxypropionate                                                  
                   70.0                                                   
______________________________________                                    
Results: The formulation of Example 3 removed paint equally as fast as the formulation of Example 1, and has the advantage that it leaves no residue on air drying, and thus may advantageously be employed in the electronics industry. On the other hand, the formulation of Examples 1 and 2 will not adhere.
It is apparent that there has been provided in accordance with the invention a paint stripper formulation and a method of making and using the same. It will be readily appreciated that the composition and method of the present invention overcome the disadvantages associated with the prior art methylene chloride-based paint strippers.
The composition has a long work life which typically permits complete removal from the substrate with a single application regardless of the thickness of the paint accumulation. In most instances, since the stripper can be left on until all the paint is loosened. Indeed, many coatings will totally dissolve if soaked. This is a significant advantage of the present invention as compared to methylene chloride paint strippers.
The paints upon which the paint stripper of the present invention is effective include those conventionally used as automotive touch-up paints, metal enamels, lacquers, varnishes, polymer paints and others used in industrial processes and also general purpose household paints and surface coatings. In addition, the stripping formulations of this invention can remove many of the dyes and pigments associated with lipstick and crayon formulations which makes this formulation highly desirable for removing graffiti where the composition of the graffiti is unknown. The stripping composition of the present invention also can be applied to reactive-vehicle or solvent borne coatings, and has also proven effective for cleaning urethane, polyester and epoxy compounds off of tools, molds, etc., particularly if applied before the cure is complete. The composition also may be emulsified with water and remain effective on many latex coatings. Emulsions in the range of 70 parts to 30 parts of water to 30 parts of the inventive formulation to 70 parts of water, are particularly useful. While the invention has been described in conjunction with several specific embodiments, it is evident that many alternatives, modifications, and variations of the invention will be apparent in light of the foregoing description. Accordingly, it is intended to embrace all such alternatives, modifications, and variations as fall within the spirit and broad scope of the appended claims.

Claims (6)

What is claimed is:
1. A non-toxic, biodegradable and ambient temperature non-volatile liquid paint stripping composition, wherein the active ingredient consists essentially of the combination of:
(a) at least 30-90% by weight of a five membered ring lactam;
(b) at least 10-70% by weight of an oxygenated aliphatic solvent selected from the group consisting of the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, hexyl, heptyl and octyl esters of 3-ethoxypropionic acid;
(c) about 0-10% by weight of a viscosifying agent selected from the group consisting of cellulose ether thickeners containing an etherifying group selected from hydroxyalkyl groups and groups derived therefrom, such etherifying groups containing 5 or 6 carbon atoms;
(d) about 0-5% by weight of a nonionic, anionic, cationic or amphoteric surface active agent; and
(e) about 0-1% by weight of a dye.
2. The composition of claim 1, wherein said five membered ring lactam comprises a lactam selected from the group consisting of N-methyl-2-pyrrolidone, N-ethyl-2-pyrrolidone, 2-hydroxy-ethyl-2-pyrrolidone, N-dimethylaminopropyl-2-pyrrolidone, vinyl-pyrrolidone, 2-pyrrolidone and mixtures thereof.
3. The composition of claim 1 wherein said lactam is N-methyl-2-pyrrolidone and is present in an amount of at least 30-40% by weight.
4. The composition of claim 1, wherein said oxygenated solvent comprises ethyl-3-ethoxypropionate and is present in an amount from about 55-75% by weight.
5. The composition of claim 1, wherein said oxygenated aliphatic solvent comprises ethyl-3-ethoxypropionate and is present in an amount of at least 65% by weight.
6. A method of stripping paint from a substrate surface which comprises the steps of:
(a) treating at room temperature the substrate surface with the composition of claim 1;
(b) allowing the composition to dwell on the surface for a sufficient period of time to degrade the paint; and
(c) removing the degraded paint by mechanical means or with pressurized stream of water.
US07/675,286 1989-08-24 1991-03-26 Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate Expired - Lifetime US5049314A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US07/675,286 US5049314A (en) 1989-08-24 1991-03-26 Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US39805289A 1989-08-24 1989-08-24
US07/675,286 US5049314A (en) 1989-08-24 1991-03-26 Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US39805289A Continuation 1989-08-24 1989-08-24

Publications (1)

Publication Number Publication Date
US5049314A true US5049314A (en) 1991-09-17

Family

ID=27016099

Family Applications (1)

Application Number Title Priority Date Filing Date
US07/675,286 Expired - Lifetime US5049314A (en) 1989-08-24 1991-03-26 Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate

Country Status (1)

Country Link
US (1) US5049314A (en)

Cited By (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5098592A (en) * 1990-10-01 1992-03-24 Creative Technologies Group, Inc. Method of activating n-methyl-2-pyrrolidone (nmp) and/or delta-butyrolactone (blo) varnish and paint remover solvents
US5154848A (en) * 1990-10-01 1992-10-13 Verona Inc. Method of activating N-methyl-2-pyrrolidone (NMP) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US5217640A (en) * 1990-10-01 1993-06-08 Verona Inc. Method of activating α-butyrolactone (BLO) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US5232515A (en) * 1991-09-19 1993-08-03 Arco Chemical Technology, L.P. Water-reducible coating removers containing n-methyl-2-pyrrolidone
US5334256A (en) * 1993-06-02 1994-08-02 Howe Charles R Paint stripping composition
US5354492A (en) * 1992-09-04 1994-10-11 Cook Composites And Polymers Company Aqueous cleaning solutions for removing uncured urethane resin systems from the surfaces of processing equipment
US5456853A (en) * 1993-04-23 1995-10-10 Rust-Oleum Corporation Paint stripping composition based on tetrahydrofurfuryl alcohol and oxygenated aliphatic solvents
WO1996040852A1 (en) * 1995-06-07 1996-12-19 Furniture Medic, Inc. Composition for stripping surfaces
US5746836A (en) * 1993-10-07 1998-05-05 Oyentos Corporation Method for removing a photosensitive layer from a photosensitive drum
US5753603A (en) * 1992-06-02 1998-05-19 Elf Atochem S.A. Paint stripping composition
US5910369A (en) * 1992-05-01 1999-06-08 American Polymer, Inc. Methods for protecting substrates with urethane protective coatings
US5916861A (en) * 1998-08-17 1999-06-29 Lyssy; Walter J. Paint stripping composition methanol and ethyl 3 ethoxypropionate
US6001192A (en) * 1992-06-02 1999-12-14 Elf Atochem S.A. Paint stripping composition
US6017862A (en) * 1997-09-29 2000-01-25 Kyzen Corporation Cleaning compositions and methods for cleaning resin and polymeric materials used in manufacture
US6635608B1 (en) * 1997-06-12 2003-10-21 Ithiel Mogridge Interior textured coating remover composition
US6669991B2 (en) * 2002-03-22 2003-12-30 Alan Stuart Method and composition for rejuvenating weathered polymeric materials
US20060186379A1 (en) * 2005-02-10 2006-08-24 Coleman Kenneth C Composition and method using same to remove urethane products from a substrate
US20070129276A1 (en) * 2005-11-17 2007-06-07 Albright Robert L Color changing paint and varnish remover
US20070272275A1 (en) * 2006-05-26 2007-11-29 Air Products And Chemicals, Inc. Composition and Method for Photoresist Removal
US20080163787A1 (en) * 2007-01-08 2008-07-10 Enthone Inc. Organic solderability preservative comprising high boiling temperature alcohol
CN101195968B (en) * 2007-12-13 2010-06-09 常熟理工学院 Treatment method of polyester fiber high temperature printing and dyeing stripping
US20120046212A1 (en) * 2009-01-23 2012-02-23 Rhodia Operations Stripping composition
US11214762B2 (en) * 2019-08-05 2022-01-04 Chem-Trend Limited Partnership Compositions and methods for cleaning urethane molds

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4401747A (en) * 1982-09-02 1983-08-30 J. T. Baker Chemical Company Stripping compositions and methods of stripping resists
US4666626A (en) * 1986-03-21 1987-05-19 C.L.M., Inc. Paint stripper compositions
WO1987007628A1 (en) * 1986-06-13 1987-12-17 Cps Kemi Aps A liquid for removing printing and screen printing inks
US4780235A (en) * 1987-04-16 1988-10-25 E. I. Du Pont De Nemours And Company Paint remover
US4788002A (en) * 1986-01-27 1988-11-29 King Lloyd H Sr Solvent cement
US4791043A (en) * 1983-12-20 1988-12-13 Hmc Patents Holding Co., Inc. Positive photoresist stripping composition
US4836950A (en) * 1984-12-14 1989-06-06 Cps Kemi Aps Liquid for removing printing and screen printing inks: butyrolactone and/or N-methyl-2-pyrrolidone and propylene glycol derivative
JPH01188311A (en) * 1988-01-22 1989-07-27 Neos Co Ltd Cleaning agent for mold

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4401747A (en) * 1982-09-02 1983-08-30 J. T. Baker Chemical Company Stripping compositions and methods of stripping resists
US4791043A (en) * 1983-12-20 1988-12-13 Hmc Patents Holding Co., Inc. Positive photoresist stripping composition
US4836950A (en) * 1984-12-14 1989-06-06 Cps Kemi Aps Liquid for removing printing and screen printing inks: butyrolactone and/or N-methyl-2-pyrrolidone and propylene glycol derivative
US4788002A (en) * 1986-01-27 1988-11-29 King Lloyd H Sr Solvent cement
US4666626A (en) * 1986-03-21 1987-05-19 C.L.M., Inc. Paint stripper compositions
WO1987007628A1 (en) * 1986-06-13 1987-12-17 Cps Kemi Aps A liquid for removing printing and screen printing inks
US4780235A (en) * 1987-04-16 1988-10-25 E. I. Du Pont De Nemours And Company Paint remover
JPH01188311A (en) * 1988-01-22 1989-07-27 Neos Co Ltd Cleaning agent for mold

Cited By (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992006169A1 (en) * 1990-10-01 1992-04-16 Verona Inc. METHOD OF ACTIVATING N-METHYL-2-PYRROLIDONE (NMP) AND/OR η-BUTYROLACTONE (BLO) VARNISH AND PAINT REMOVER SOLVENTS
US5154848A (en) * 1990-10-01 1992-10-13 Verona Inc. Method of activating N-methyl-2-pyrrolidone (NMP) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US5217640A (en) * 1990-10-01 1993-06-08 Verona Inc. Method of activating α-butyrolactone (BLO) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US5098592A (en) * 1990-10-01 1992-03-24 Creative Technologies Group, Inc. Method of activating n-methyl-2-pyrrolidone (nmp) and/or delta-butyrolactone (blo) varnish and paint remover solvents
US5232515A (en) * 1991-09-19 1993-08-03 Arco Chemical Technology, L.P. Water-reducible coating removers containing n-methyl-2-pyrrolidone
US6312815B1 (en) 1992-05-01 2001-11-06 American Polymer Corporation Two layer protective coatings
US5910369A (en) * 1992-05-01 1999-06-08 American Polymer, Inc. Methods for protecting substrates with urethane protective coatings
US5753603A (en) * 1992-06-02 1998-05-19 Elf Atochem S.A. Paint stripping composition
US6001192A (en) * 1992-06-02 1999-12-14 Elf Atochem S.A. Paint stripping composition
US5354492A (en) * 1992-09-04 1994-10-11 Cook Composites And Polymers Company Aqueous cleaning solutions for removing uncured urethane resin systems from the surfaces of processing equipment
US5456853A (en) * 1993-04-23 1995-10-10 Rust-Oleum Corporation Paint stripping composition based on tetrahydrofurfuryl alcohol and oxygenated aliphatic solvents
US5334256A (en) * 1993-06-02 1994-08-02 Howe Charles R Paint stripping composition
US5746836A (en) * 1993-10-07 1998-05-05 Oyentos Corporation Method for removing a photosensitive layer from a photosensitive drum
WO1996040852A1 (en) * 1995-06-07 1996-12-19 Furniture Medic, Inc. Composition for stripping surfaces
US6635608B1 (en) * 1997-06-12 2003-10-21 Ithiel Mogridge Interior textured coating remover composition
US6017862A (en) * 1997-09-29 2000-01-25 Kyzen Corporation Cleaning compositions and methods for cleaning resin and polymeric materials used in manufacture
US5916861A (en) * 1998-08-17 1999-06-29 Lyssy; Walter J. Paint stripping composition methanol and ethyl 3 ethoxypropionate
US6669991B2 (en) * 2002-03-22 2003-12-30 Alan Stuart Method and composition for rejuvenating weathered polymeric materials
US7531049B2 (en) 2005-02-10 2009-05-12 Danny P. Tepolt Composition and method using same to remove urethane products from a substrate
US20060186379A1 (en) * 2005-02-10 2006-08-24 Coleman Kenneth C Composition and method using same to remove urethane products from a substrate
US20070129276A1 (en) * 2005-11-17 2007-06-07 Albright Robert L Color changing paint and varnish remover
US8383565B2 (en) * 2005-11-17 2013-02-26 Sunnyside Corporation Color changing paint and varnish remover
US20070272275A1 (en) * 2006-05-26 2007-11-29 Air Products And Chemicals, Inc. Composition and Method for Photoresist Removal
US8288330B2 (en) * 2006-05-26 2012-10-16 Air Products And Chemicals, Inc. Composition and method for photoresist removal
US20080163787A1 (en) * 2007-01-08 2008-07-10 Enthone Inc. Organic solderability preservative comprising high boiling temperature alcohol
US7794531B2 (en) 2007-01-08 2010-09-14 Enthone Inc. Organic solderability preservative comprising high boiling temperature alcohol
CN101195968B (en) * 2007-12-13 2010-06-09 常熟理工学院 Treatment method of polyester fiber high temperature printing and dyeing stripping
US20120046212A1 (en) * 2009-01-23 2012-02-23 Rhodia Operations Stripping composition
US9376578B2 (en) * 2009-01-23 2016-06-28 Rhodia Operations Stripping composition
US11214762B2 (en) * 2019-08-05 2022-01-04 Chem-Trend Limited Partnership Compositions and methods for cleaning urethane molds

Similar Documents

Publication Publication Date Title
US5049314A (en) Paint stripping composition consisting essentially of NMP and ethyl-3-ethoxy propionate
US4812255A (en) Paint removing compositions
US5334331A (en) Method of activating N-methyl-2-pyrrolidone (NMP) varnish and paint remover solvents for removal of organic coatings
US5035829A (en) Paint removing compositions
US5215675A (en) Aqueous stripping composition containing peroxide and water soluble ester
US5565136A (en) Water based wood stripping compositions
US5310496A (en) Vegetable oil based paint removing compositions
EP1175462B1 (en) Paint and coating remover
US5011621A (en) Paint stripper compositions containing N-methyl-2-pyrrolidone and renewable resources
US6191087B1 (en) Environmentally friendly solvent
CA2803389C (en) Carboxy ester ketal removal compositions, methods of manufacture, and uses thereof
US6159915A (en) Paint and coating remover
US5049300A (en) Method of activating acidified NMP to provide an effective paint remover composition
CA2063739C (en) Method of activating n-methyl-e-pyrrolidone (nmp) and/or gamma-butyrolactone (blo) varnish and paint remover solvents
EP1313815A2 (en) Paint stripping compositions
US5456853A (en) Paint stripping composition based on tetrahydrofurfuryl alcohol and oxygenated aliphatic solvents
US8603258B2 (en) Paint and ink remover two-phase system
US5154848A (en) Method of activating N-methyl-2-pyrrolidone (NMP) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
US6030466A (en) Paint stripping composition based on tetrahydrofurfuryl ethers
CA1320675C (en) Paint stripping composition containing five membered ring lactone
WO2016014763A1 (en) Mixed solvent based compositions for removal of paint and varnish
US5217640A (en) Method of activating α-butyrolactone (BLO) with ethyl 3-ethoxypropionate (EEP) to provide improved varnish and paint remover solvents
DK169079B1 (en) Essentially anhydrous agent for the laceration of blanks of easily corroded materials containing N-methyl-pyrrolidone, potassium hydroxide and an alcohol of 2-3 carbon atoms, and process for its preparation and use thereof.
US5472641A (en) Single phase aqueous paint remover compositions including trioxane, water and an organic co-solvent
NO884633L (en) COMPOSITIONS FOR REMOVING PAINT.

Legal Events

Date Code Title Description
STCF Information on status: patent grant

Free format text: PATENTED CASE

AS Assignment

Owner name: MARGARET VILLA INC., MAINE

Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:CHUTE CHEMICAL COMPANY;REEL/FRAME:006617/0534

Effective date: 19930608

FEPP Fee payment procedure

Free format text: PAYOR NUMBER ASSIGNED (ORIGINAL EVENT CODE: ASPN); ENTITY STATUS OF PATENT OWNER: SMALL ENTITY

FPAY Fee payment

Year of fee payment: 4

FPAY Fee payment

Year of fee payment: 8

FPAY Fee payment

Year of fee payment: 12